Canonical Allele Identifier: PA2826059709
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 706220
ClinVar RCV Id: RCV000876757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Glu152Asp
CA10321202
NM_001169111.2:c.456A>T
CA412192666
NM_001169111.2:c.456A>C